Light-dependent translocation of arrestin in rod photoreceptors is signaled through a phospholipase C cascade and requires ATP
- Publication type:
- Journal article
- Metadata:
-
- Autoren
- Wilda Orisme
- Jian Li
- Tobias Goldmann
- Susan Bolch
- Uwe Wolfrum
- W Clay Smith
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000273935700012&DestLinkType=FullRecord&DestApp=WOS_CPL
- DOI
- 10.1016/j.cellsig.2009.10.016
- eISSN
- 1873-3913
- Externe Identifier
- Clarivate Analytics Document Solution ID: 548CD
- PubMed Identifier: 19887106
- ISSN
- 0898-6568
- Ausgabe der Veröffentlichung
- 3
- Zeitschrift
- CELLULAR SIGNALLING
- Schlüsselwörter
- Arrestin
- Translocation
- G-protein
- Phosphoinositides
- Protein kinase C
- Rod photoreceptors
- Paginierung
- 447 - 456
- Datum der Veröffentlichung
- 2010
- Status
- Published
- Titel
- Light-dependent translocation of arrestin in rod photoreceptors is signaled through a phospholipase C cascade and requires ATP
- Sub types
- Article
- Ausgabe der Zeitschrift
- 22
Data source: Web of Science (Lite)
- Other metadata sources:
-
- Autoren
- Wilda Orisme
- Jian Li
- Tobias Goldmann
- Susan Bolch
- Uwe Wolfrum
- W Clay Smith
- DOI
- 10.1016/j.cellsig.2009.10.016
- ISSN
- 0898-6568
- Ausgabe der Veröffentlichung
- 3
- Zeitschrift
- Cellular Signalling
- Sprache
- en
- Paginierung
- 447 - 456
- Datum der Veröffentlichung
- 2010
- Status
- Published
- Herausgeber
- Elsevier BV
- Herausgeber URL
- http://dx.doi.org/10.1016/j.cellsig.2009.10.016
- Datum der Datenerfassung
- 2021
- Titel
- Light-dependent translocation of arrestin in rod photoreceptors is signaled through a phospholipase C cascade and requires ATP
- Ausgabe der Zeitschrift
- 22
Data source: Crossref
- Abstract
- Partitioning of cellular components is a critical mechanism by which cells can regulate their activity. In rod photoreceptors, light induces a large-scale translocation of arrestin from the inner segments to the outer segments. The purpose of this project is to elucidate the signaling pathway necessary to initiate arrestin translocation to the outer segments and the mechanism for arrestin translocation. Mouse retinal organotypic cultures and eyes from transgenic Xenopus tadpoles expressing a fusion of GFP and rod arrestin were treated with both activators and inhibitors of proteins in the phosphoinositide pathway. Confocal microscopy was used to image the effects of the pharmacological agents on arrestin translocation in rod photoreceptors. Retinas were also depleted of ATP using potassium cyanide to assess the requirement for ATP in arrestin translocation. In this study, we demonstrate that components of the G-protein-linked phospholipase C (PLC) pathway play a role in initiating arrestin translocation. Our results show that arrestin translocation can be stimulated by activators of PLC and protein kinase C (PKC), and by cholera toxin in the absence of light. Arrestin translocation to the outer segments is significantly reduced by inhibitors of PLC and PKC. Importantly, we find that treatment with potassium cyanide inhibits arrestin translocation in response to light. Collectively, our results suggest that arrestin translocation is initiated by a G-protein-coupled cascade through PLC and PKC signaling. Furthermore, our results demonstrate that at least the initiation of arrestin translocation requires energy input.
- Addresses
- Department of Ophthalmology, University of Florida, Gainesville, Florida 32610-0284, USA.
- Autoren
- Wilda Orisme
- Jian Li
- Tobias Goldmann
- Tobias Goldmann
- Susan Bolch
- Uwe Wolfrum
- W Clay Smith
- DOI
- 10.1016/j.cellsig.2009.10.016
- eISSN
- 1873-3913
- Externe Identifier
- PubMed Identifier: 19887106
- PubMed Central ID: PMC2794968
- Funding acknowledgements
- NEI NIH HHS: EY08571
- NEI NIH HHS: P30 EY021721
- NEI NIH HHS: R01 EY014864
- FAUN-Stiftung, Nürnberg, Germany:
- National Eye Institute: EY014864
- Deutsche Forschungsgemeinschaft: GRK1044
- NEI NIH HHS: R01 EY006225
- NEI NIH HHS: R01 EY006225-24
- NEI NIH HHS: T32 EY007132-17
- NEI NIH HHS: EY007132
- NEI NIH HHS: EY014864
- NEI NIH HHS: T32 EY007132
- Research to Prevent Blindness:
- NEI NIH HHS: P30 EY008571
- National Eye Institute: EY06225
- National Eye Institute: EY08571
- NEI NIH HHS: P30 EY008571-20
- NEI NIH HHS: R01 EY014864-05
- Karl Kirchgessner Foundation:
- National Eye Institute: EY007132
- NEI NIH HHS: EY06225
- Open access
- false
- ISSN
- 0898-6568
- Ausgabe der Veröffentlichung
- 3
- Zeitschrift
- Cellular signalling
- Schlüsselwörter
- Cells, Cultured
- Animals
- Xenopus laevis
- Mice
- Potassium Cyanide
- Cholera Toxin
- Protein Kinase C
- Phosphatidylinositols
- Arrestin
- Adenosine Triphosphate
- Enzyme Inhibitors
- Signal Transduction
- Light
- Type C Phospholipases
- Retinal Rod Photoreceptor Cells
- Sprache
- eng
- Medium
- Paginierung
- 447 - 456
- Datum der Veröffentlichung
- 2010
- Status
- Published
- Datum der Datenerfassung
- 2009
- Titel
- Light-dependent translocation of arrestin in rod photoreceptors is signaled through a phospholipase C cascade and requires ATP.
- Sub types
- Research Support, Non-U.S. Gov't
- research-article
- Journal Article
- Research Support, N.I.H., Extramural
- Ausgabe der Zeitschrift
- 22
Data source: Europe PubMed Central
- Abstract
- Partitioning of cellular components is a critical mechanism by which cells can regulate their activity. In rod photoreceptors, light induces a large-scale translocation of arrestin from the inner segments to the outer segments. The purpose of this project is to elucidate the signaling pathway necessary to initiate arrestin translocation to the outer segments and the mechanism for arrestin translocation. Mouse retinal organotypic cultures and eyes from transgenic Xenopus tadpoles expressing a fusion of GFP and rod arrestin were treated with both activators and inhibitors of proteins in the phosphoinositide pathway. Confocal microscopy was used to image the effects of the pharmacological agents on arrestin translocation in rod photoreceptors. Retinas were also depleted of ATP using potassium cyanide to assess the requirement for ATP in arrestin translocation. In this study, we demonstrate that components of the G-protein-linked phospholipase C (PLC) pathway play a role in initiating arrestin translocation. Our results show that arrestin translocation can be stimulated by activators of PLC and protein kinase C (PKC), and by cholera toxin in the absence of light. Arrestin translocation to the outer segments is significantly reduced by inhibitors of PLC and PKC. Importantly, we find that treatment with potassium cyanide inhibits arrestin translocation in response to light. Collectively, our results suggest that arrestin translocation is initiated by a G-protein-coupled cascade through PLC and PKC signaling. Furthermore, our results demonstrate that at least the initiation of arrestin translocation requires energy input.
- Date of acceptance
- 2009
- Autoren
- Wilda Orisme
- Jian Li
- Tobias Goldmann
- Susan Bolch
- Uwe Wolfrum
- W Clay Smith
- Autoren-URL
- https://www.ncbi.nlm.nih.gov/pubmed/19887106
- DOI
- 10.1016/j.cellsig.2009.10.016
- eISSN
- 1873-3913
- Externe Identifier
- NIH Manuscript Submission ID: NIHMS156715
- PubMed Central ID: PMC2794968
- Funding acknowledgements
- NEI NIH HHS: EY08571
- NEI NIH HHS: EY014864
- NEI NIH HHS: R01 EY014864
- NEI NIH HHS: EY06225
- NEI NIH HHS: R01 EY014864-05
- NEI NIH HHS: R01 EY006225-24
- NEI NIH HHS: T32 EY007132-17
- NEI NIH HHS: T32 EY007132
- NEI NIH HHS: P30 EY008571
- NEI NIH HHS: P30 EY021721
- NEI NIH HHS: P30 EY008571-20
- NEI NIH HHS: EY007132
- NEI NIH HHS: R01 EY006225
- Ausgabe der Veröffentlichung
- 3
- Zeitschrift
- Cell Signal
- Schlüsselwörter
- Adenosine Triphosphate
- Animals
- Arrestin
- Cells, Cultured
- Cholera Toxin
- Enzyme Inhibitors
- Light
- Mice
- Phosphatidylinositols
- Potassium Cyanide
- Protein Kinase C
- Retinal Rod Photoreceptor Cells
- Signal Transduction
- Type C Phospholipases
- Xenopus laevis
- Sprache
- eng
- Country
- England
- Paginierung
- 447 - 456
- PII
- S0898-6568(09)00333-7
- Datum der Veröffentlichung
- 2010
- Status
- Published
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2010
- Titel
- Light-dependent translocation of arrestin in rod photoreceptors is signaled through a phospholipase C cascade and requires ATP.
- Sub types
- Journal Article
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't
- Ausgabe der Zeitschrift
- 22
Data source: PubMed
- Beziehungen:
- Property of